Valerie D. Hipkins
United States Forest Service
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Featured researches published by Valerie D. Hipkins.
Molecular Ecology | 2008
Karen E. Mock; Carol A. Rowe; Mevin B. Hooten; Jennifer DeWoody; Valerie D. Hipkins
Clonality is a common phenomenon in plants, allowing genets to persist asexually for much longer periods of time than ramets. The relative frequency of sexual vs. asexual reproduction determines long‐term dominance and persistence of clonal plants at the landscape scale. One of the most familiar and valued clonal plants in North America is aspen (Populus tremuloides). Previous researchers have suggested that aspen in xeric landscapes of the intermountain west represent genets of great chronological age, maintained via clonal expansion in the near absence of sexual reproduction. We synthesized microsatellite data from 1371 ramets in two large sampling grids in Utah. We found a surprisingly large number of distinct genets, some covering large spatial areas, but most represented by only one to a few individual ramets at a sampling scale of 50 m. In general, multi‐ramet genets were spatially cohesive, although some genets appear to be fragmented remnants of much larger clones. We conclude that recent sexual reproduction in these landscapes is a stronger contributor to standing genetic variation at the population level than the accumulation of somatic mutations, and that even some of the spatially large clones may not be as ancient as previously supposed. Further, a striking majority of the largest genets in both study areas had three alleles at one or more loci, suggesting triploidy or aneuploidy. These genets tended to be spatially clustered but not closely related. Together, these findings substantially advance our understanding of clonal dynamics in western North American aspen, and set the stage for a broad range of future studies.
Tree Genetics & Genomes | 2015
Kevin M. Potter; Valerie D. Hipkins; Mary F. Mahalovich; Robert E. Means
Ponderosa pine (Pinus ponderosa) is among the most broadly distributed conifer species of western North America, where it possesses considerable ecological, esthetic, and commercial value. It exhibits complicated patterns of morphological and genetic variation, suggesting that it may be in the process of differentiating into distinct regional lineages. A robust analysis of genetic variation across the ponderosa pine complex is necessary to ensure the effectiveness of management and conservation efforts given the species’ large distribution, the existence of many isolated disjunct populations, and the potential susceptibility of some populations to climate change and other threats. We used highly polymorphic nuclear microsatellite markers and isozyme markers from 3113 trees in 104 populations to assess genetic variation and structure across the geographic range of ponderosa pine. The results reveal pervasive inbreeding and patterns of genetic diversity consistent with the hypothesis that ponderosa existed in small, as-yet-undetected Pleistocene glacial refugia north of southern Arizona and New Mexico. The substructuring of genetic variation within the species complex was consistent with its division into two varieties, with genetic clusters within varieties generally associated with latitudinal zones. The analyses indicate widespread gene flow and/or recent common ancestry among genetic clusters within varieties, but not between varieties. Isolated disjunct populations had lower genetic variation by some measures and greater genetic differentiation than main-range populations. These results should be useful for decision-making and conservation planning related to this widespread and important species.
Western North American Naturalist | 2008
Jennifer DeWoody; Carol A. Rowe; Valerie D. Hipkins; Karen E. Mock
Abstract While clones of trembling aspen (Populus tremuloides, Michx.) in the Intermountain West of North America are expected to be large, one putative genet in central Utah, identified from morphological evidence, has garnered particular attention for its size, even gaining the nickname “Pando” (Latin for “I spread”). In order to determine if a single genetic individual coincides with the morphological boundary of “Pando,” we sampled 209 stems on a 50-m grid throughout the putative clone for analysis at 7 microsatellite loci. We have identified a single genetic entity concurrent with that described from morphological characteristics. Spatial analyses indicate that the clone covers approximately 43.6 ha. Surprisingly, an additional 40 genotypes were identified adjacent to the putative clone, indicating that genet diversity may be high in the stand as a whole. In confirming the existence of the “Pando” clone, we suggest that this organism will provide valuable opportunities to study important biological processes such as clonal growth, somatic mutation, and senescence.
International Journal of Plant Sciences | 2009
W. S. Dvorak; Kevin M. Potter; Valerie D. Hipkins; Gary R. Hodge
Eleven highly polymorphic microsatellite markers were used to determine the genetic structure and levels of diversity in 51 natural populations of Pinus oocarpa across its geographic range of 3000 km in Mesoamerica. The study also included 17 populations of Pinus patula and Pinus tecunumanii chosen for their resistance or susceptibility to the pitch canker fungus based on previous research. Seedlings from all 68 populations were screened for pitch canker resistance, and results were correlated to mean genetic diversity and collection site variables. Results indicate that P. oocarpa exhibits average to above‐average levels of genetic diversity ( \documentclass{aastex} \usepackage{amsbsy} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{bm} \usepackage{mathrsfs} \usepackage{pifont} \usepackage{stmaryrd} \usepackage{textcomp} \usepackage{portland,xspace} \usepackage{amsmath,amsxtra} \usepackage[OT2,OT1]{fontenc} \newcommand\cyr{ \renewcommand\rmdefault{wncyr} \renewcommand\sfdefault{wncyss} \renewcommand\encodingdefault{OT2} \normalfont \selectfont} \DeclareTextFontCommand{\textcyr}{\cyr} \pagestyle{empty} \DeclareMathSizes{10}{9}{7}{6} \begin{document} \landscape
Tree Genetics & Genomes | 2009
Konstantin V. Krutovsky; John Bradley St. Clair; Robert Saich; Valerie D. Hipkins; David B. Neale
Conservation Genetics | 2012
Kevin M. Potter; Robert M. Jetton; W. S. Dvorak; Valerie D. Hipkins; Rusty Rhea; W. Andrew Whittier
A=19.82
American Journal of Botany | 2013
Kevin M. Potter; Valerie D. Hipkins; Mary F. Mahalovich; Robert E. Means
Tree Genetics & Genomes | 2006
Nicholas C. Wheeler; Peggy Payne; Valerie D. Hipkins; Robert Saich; Stephen Kenny; Gerald A. Tuskan
\end{document} , \documentclass{aastex} \usepackage{amsbsy} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{bm} \usepackage{mathrsfs} \usepackage{pifont} \usepackage{stmaryrd} \usepackage{textcomp} \usepackage{portland,xspace} \usepackage{amsmath,amsxtra} \usepackage[OT2,OT1]{fontenc} \newcommand\cyr{ \renewcommand\rmdefault{wncyr} \renewcommand\sfdefault{wncyss} \renewcommand\encodingdefault{OT2} \normalfont \selectfont} \DeclareTextFontCommand{\textcyr}{\cyr} \pagestyle{empty} \DeclareMathSizes{10}{9}{7}{6} \begin{document} \landscape
New Forests | 2017
Kevin M. Potter; Robert M. Jetton; Andrew D. Bower; Douglass F. Jacobs; Gary Man; Valerie D. Hipkins; Murphy Westwood
PLOS ONE | 2016
Douglas J. Shinneman; Robert E. Means; Kevin M. Potter; Valerie D. Hipkins
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